A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100590



Internal ID22009823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128694773..128694863hg38UCSC Ensembl
chr9:131457052..131457142hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578970
Samples
Known GenesSET
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100590
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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